HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2265092Generated: October 28, 2026
p-Nitroacetophenone → HCID 11031413, compound
https://huagongshe.com/reaction/2265092
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | p-Nitroacetophenone | HCID 7487 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 18-Crown-6 | HCID 28557 | — |
| Reactant | Trimethyl phosphonoacetate | HCID 80029 | — |
| Reactant | Potassium bis(trimethylsilyl)amide | HCID 3251421 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 11031413 | HCID 11031413 | 46% |
Reaction Steps
18-Crown-6 (41.6 g) was added to a toluene (484 ml) solution of trimethyl phosphonoacetate (22.6 ml) in a nitrogen atmosphere. An 11% potassium hexamethyldisilazide (hereinafter referred to as “KHMDS”)/toluene solution (315 ml) was added thereto, and the obtained mixture was stirred for 1 hour. Under ice-cooling, 4-nitroacetophenone (20 g) was added thereto, and the mixture was stirred for 1 hour. After the reaction was over, the reaction was stopped with a saturated ammonium chloride solution. The reaction mixture was separated with ethyl acetate and water. The organic layer was washed three times with water and once with a saturated sodium chloride solution, and then dried over anhydrous sodium sulfate. After the solvent was distilled off, the residue was suspended in methanol (40 ml) and stirred. The precipitated solid was filtered off and washed with cold methanol. Thus, Compound 6a (12.4 g, 46%) was obtained as an opalescent solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07855300B2 |
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| Source dataset | uspto-grants-2010_12 |
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| ORD ID | ord-4e1abc231d0e4d6fb1cb0ef1bce0716c |
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| Source note | uspto-grants-2010_12 |
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